Canonical Allele Identifier: PA1139756692
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 993903
ClinVar RCV Id: RCV001297304 RCV001812962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Cys11Trp
CA398535465
NM_144997.7:c.33C>G